SYPHILIS / TP test - India CDSCO Medical Device Registration
SYPHILIS / TP test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000020_84fb0400ab2fcd1abaafe023e3b6b338_1ed87db04562a67637f534803eef93ac. The license holder is Koshbio Private Limited, and it is classified as Device Class Class D. The approving authority is Sub Zonal Baddi.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
License Holder
Koshbio Private LimitedDevice Class
Approving Authority
Sub Zonal Baddi
Product Information
SYPHILIS / TP test is a rapid card test based upon immuno-chromatography principle for the qualitative detection of IgM / IgG / IgA antibodies of Treponema pallidum (NA) in human specimen to an aid in the diagnosis of infection with Treponema pallidum or Syphilis. For professional and in-vitro diagnostic use only.
